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| Status |
Public on Jan 07, 2013 |
| Title |
IgG ChIP-seq (10T1/2) |
| Sample type |
SRA |
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| Source name |
C3H10T1/2 mouse cells
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| Organism |
Mus musculus |
| Characteristics |
cell type: C3H10T1/2 cells
chip antibody: IgG (in-house)
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| Growth protocol |
Cell culture protocol: C3H10T1/2, C2C12 cells were cultured in high glucose DMEM with 10% fetal bovine serum at 10% CO2.
Adipogenesis protocol: For adipogenesis, cells were grown to confluence in medium containing 10% fetal bovine serum. At confluence, cells were exposed to induction medium containing dexamethasone (1uM), IBMX(0.1mM), insulin(5ug/ml) and rosiglitazone(1uM), and 10% FBS. 3 days later, cells were further cultured in DMEM containing insulin (5ug/ml) and rosiglitazone (1uM) until they were ready for collection.
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| Extracted molecule |
genomic DNA |
| Extraction protocol |
Antibody production and purification, antibodies: A fragment of the TAF7L gene corresponding to residues 500-600 was cloned into the pGEX-4T-1 vector carrying a GST tag. GST-TAF7L was expressed and purified from E.coli and injected into rabbits. Bleeds were collected after three boosts and TAF7L antibodies were tested and confirmed by in vitro transcribed and translated TAF7L and mouse testis whole protein extracts from wild-type and TAF7L knockout mice. The antisera obtained were affinity-purified using antigen immobilized on Affigel 10/15 resin (Bio-rad). For Pol II antibody, monoclonal anti-Pol II (8WG16) was concentrated from hybridoma supernatant with Protein A Sepharose Beads (GE Healthcare).
ChIP, ChIP libraries preparation, and deep sequencing (ChIP-seq): Fix C3H10T1/2 cells and differentiated adipocytes with 1% formaldehyde for 10 mins at room temperature then use 0.125M glycine to stop the crosslinking for an additional 5 mins. Collect cells and extract nuclei with extraction buffer. The chromatin obtained from C3H10T1/2 cells and adipocytes was fragmented to sizes ranging from 175 to 250 bp using a Covaris-S2 (Covaris, Inc.) sonicator for a total processing time of 40 min (20s on, 20s off). 900 µg of the chromatin was used in each immunoprecipitation reaction as previously described (Liu et al., 2011), with the Pol II, TBP, PPARγ and TAF7L antibodies, mouse and rabbit IgG as negative controls respectively. We prepared the IgG abs in-house from mice and rabbits and concentrated with Protein A Sepharose Beads (GE Healthcare).
Preparation of the ChIP-seq and mRNA-seq libraries on the DNA samples of the immunoprecipitation from antibodies and IgGs and mRNA extracted from different cells precisely followed the instructions from Illumina (Illumina Inc.), qualities of the libraries were assessed by 2100 Bioanalyzer and then subjected to ultra-high throughput sequencing.
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| Library strategy |
ChIP-Seq |
| Library source |
genomic |
| Library selection |
ChIP |
| Instrument model |
Illumina HiSeq 2000 |
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| Description |
Input ChIP-seq (10T1/2)
Sample name: HY_PI_Pre
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| Data processing |
Peak calling methods: To accurately identify significant binding positions across the genome, we incorporated two peak calling methods, as described previously (May et al., 2012). First, we used MACS (Zhang et al., 2008) (version 1.4, with default settings except: --nomodel --shiftsize=110 --pvalue=1e-2 --mfold=10,10000 --slocal=2000 --llocal=20000), with an FDR significant threshold of 0.05 (using IgG ChIP as a control). Second, we applied the Grizzly peak fitting algorithm (Harrison et al., 2011), which uses a model-based iterative approach to accurately identify multiple binding loci at every enriched region. Peaks were then associated with the nearest TSS (using gene annotation from UCSC, version mm9), and classified as promoter peaks (up to 500bp from start site), proximal enhancer peaks (larger than 500bp and less than 5Kb), distal enhancer peaks (less than 50 Kb from TSS), or none (further away than any start site). Peaks are summarized in the following format: (1) position (2) chromosome (3) from position (4) to position (5) max coverage (6) total coverage (7) peaks (8) their respective heights (9) threshold for stopping criterion. Note: There are some runs with no or very few peaks called.
Digital gene expression of mRNA-seq: The reads were than mapped to the mouse transcriptome (created using UCSC table browser, version mm9, on February 2012), using TopHat (Trapnell et al., 2009), version v1.4.0., using default parameters. We then applied cufflinks (Trapnell et al., 2010), version v1.3.0, using the default parameters except: --max-mle-iterations 1, to estimate the digital expression levels at each transcript. Due to the high number of sequence reads, these steps were done in seven batches of 25 million reads each, per sample.
Genome_build: UCSC mm9 [MGSCv37]
Supplementary_files_format_and_content: Peak calling output files (.xls; intersection of MACS and Grizzly Peak fitting algorithms).
Supplementary_files_format_and_content: Adipose_mRNA_ChIP.xlsx and Adipose_mRNA_ChIP.txt are large tables summarizing ChIP binding at promoters, proximal or remote for every data/gene, as well as gene expression levels and ratios. These two files are mostly identical: the binary excel format is ideal for visualizations and the text version suitable for automated parsing. The files were generated using my MATLAB programs, then curated manually.
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| Submission date |
Nov 02, 2012 |
| Last update date |
May 15, 2019 |
| Contact name |
Tommy Kaplan |
| E-mail(s) |
tommy@cs.huji.ac.il
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| Organization name |
Hebrew University
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| Department |
School of Computer Science and Engineering
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| Street address |
Givat Ram Campus
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| City |
Jerusalem |
| ZIP/Postal code |
91904 |
| Country |
Israel |
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| Platform ID |
GPL13112 |
| Series (1) |
| GSE41937 |
Dual Functions of TAF7L in Adipocyte Differentiation |
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| Relations |
| SRA |
SRX202793 |
| BioSample |
SAMN01798296 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSM1030540_HY_PI_Pre.xls.gz |
86 b |
(ftp)(http) |
XLS |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data provided as supplementary file |
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